HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357283Generated: October 29, 2026
Methanol → 2-[(2,6-Dichloro-3-methylphenyl)amino]benzaldehyde
https://huagongshe.com/reaction/357283
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | N-methoxy-N-methyl-2-[(2,6-dichloro-4-methylphenyl)amino]benzamide | HCID 18936985 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(2,6-Dichloro-3-methylphenyl)amino]benzaldehyde | HCID 15027377 | 63% |
Reaction Steps
To a magnetically stirred 0° C. solution in dry THF (25 mL) of N-methoxy-N-methyl-2-[(2,6-dichloro-4-methylphenyl)amino]benzamide (3.8 g, 11.2 mmol), prepared as in step 1, was added dropwise diisobutylaluminum hydride (1.0M in THF, 24.6 mL) and the reaction mixture was stirred at ambient temperature for 16 hours. Methanol (5 mL) was added dropwise and the mixture was stirred for 15 minutes until a white precipitate had formed. The reaction mixture was concentrated, the residue was taken up in methanol (10 mL), the insoluble white solid was filtered, and the filtrate was evaporated in vacuo and then purified by chromatography on silica gel (5:1 hexane/CH2Cl2) to provide 2-[(2,6-dichloro-3-methylphenyl)amino]benzaldehyde (1.98 g; 63%) and over reduced alcohol side product (0.70 g; 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840758 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-569e3f0cf38b4282a44e341e8299339e |
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| Source note | uspto-grants-1998_11 |
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